Non-Surgical Cancer Risk Reduction in <i>BRCA1 </i>Mutation Carriers: Disabling the Remote Control
Women-specific cancers are a major health issue, particularly those associated with the <i>BRCA</i><i>1</i> germline mutation carrier state, which include triple-negative basal breast carcinomas and high-grade serous ovarian carcinomas (referred to as extra-uterine Mü...
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doaj-7116f139db994709a985e3d06c72751c2020-11-25T01:19:53ZengMDPI AGCancers2072-66942020-02-0112354710.3390/cancers12030547cancers12030547Non-Surgical Cancer Risk Reduction in <i>BRCA1 </i>Mutation Carriers: Disabling the Remote ControlMartin Widschwendter0Louis Dubeau1Department of Women’s Cancer, University College London, 74 Huntley Street, London WC1E 6AU, UKDepartment of Pathology, Keck School of Medicine, USC/Norris Comprehensive Cancer Centre, University of Southern California, Los Angeles, CA 90089, USAWomen-specific cancers are a major health issue, particularly those associated with the <i>BRCA</i><i>1</i> germline mutation carrier state, which include triple-negative basal breast carcinomas and high-grade serous ovarian carcinomas (referred to as extra-uterine Müllerian carcinomas). Whereas many chronic diseases can currently be prevented (e.g., cardiovascular diseases), no recent tangible progress was made in cancer prevention of <i>BRCA1</i> mutation carriers apart from surgical resections of at-risk organs. This lack of progress is largely due to (1) poor understanding of the initiating events triggered by known risk factors in the development of these cancers, (2) the fact that current preventive measures rely on evidence obtained from adjuvant breast cancer treatment that fail to protect against poor prognostic cancers, and (3) problems with using cancer incidence in high-risk women as an ethically justifiable endpoint in cancer prevention trials. Here, we propose that cancer predisposition in BRCA1 mutation carriers is driven, at least in part, by cell-nonautonomous mechanisms (i.e., driven by consequences of this carrier state on hormonal and other systemic factors controlled in organs other than those that are cancer-prone) and that biomarkers of epigenomic reprogramming, hypothesized to be a direct consequence of such cell-nonautonomous mechanisms, are attractive as intermediate surrogate endpoints to assess the efficacy of cancer risk-reducing strategies targeting these mechanisms.https://www.mdpi.com/2072-6694/12/3/547brca1 mutationsovarian cancerbreast cancerprevention |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Martin Widschwendter Louis Dubeau |
spellingShingle |
Martin Widschwendter Louis Dubeau Non-Surgical Cancer Risk Reduction in <i>BRCA1 </i>Mutation Carriers: Disabling the Remote Control Cancers brca1 mutations ovarian cancer breast cancer prevention |
author_facet |
Martin Widschwendter Louis Dubeau |
author_sort |
Martin Widschwendter |
title |
Non-Surgical Cancer Risk Reduction in <i>BRCA1 </i>Mutation Carriers: Disabling the Remote Control |
title_short |
Non-Surgical Cancer Risk Reduction in <i>BRCA1 </i>Mutation Carriers: Disabling the Remote Control |
title_full |
Non-Surgical Cancer Risk Reduction in <i>BRCA1 </i>Mutation Carriers: Disabling the Remote Control |
title_fullStr |
Non-Surgical Cancer Risk Reduction in <i>BRCA1 </i>Mutation Carriers: Disabling the Remote Control |
title_full_unstemmed |
Non-Surgical Cancer Risk Reduction in <i>BRCA1 </i>Mutation Carriers: Disabling the Remote Control |
title_sort |
non-surgical cancer risk reduction in <i>brca1 </i>mutation carriers: disabling the remote control |
publisher |
MDPI AG |
series |
Cancers |
issn |
2072-6694 |
publishDate |
2020-02-01 |
description |
Women-specific cancers are a major health issue, particularly those associated with the <i>BRCA</i><i>1</i> germline mutation carrier state, which include triple-negative basal breast carcinomas and high-grade serous ovarian carcinomas (referred to as extra-uterine Müllerian carcinomas). Whereas many chronic diseases can currently be prevented (e.g., cardiovascular diseases), no recent tangible progress was made in cancer prevention of <i>BRCA1</i> mutation carriers apart from surgical resections of at-risk organs. This lack of progress is largely due to (1) poor understanding of the initiating events triggered by known risk factors in the development of these cancers, (2) the fact that current preventive measures rely on evidence obtained from adjuvant breast cancer treatment that fail to protect against poor prognostic cancers, and (3) problems with using cancer incidence in high-risk women as an ethically justifiable endpoint in cancer prevention trials. Here, we propose that cancer predisposition in BRCA1 mutation carriers is driven, at least in part, by cell-nonautonomous mechanisms (i.e., driven by consequences of this carrier state on hormonal and other systemic factors controlled in organs other than those that are cancer-prone) and that biomarkers of epigenomic reprogramming, hypothesized to be a direct consequence of such cell-nonautonomous mechanisms, are attractive as intermediate surrogate endpoints to assess the efficacy of cancer risk-reducing strategies targeting these mechanisms. |
topic |
brca1 mutations ovarian cancer breast cancer prevention |
url |
https://www.mdpi.com/2072-6694/12/3/547 |
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AT martinwidschwendter nonsurgicalcancerriskreductioninibrca1imutationcarriersdisablingtheremotecontrol AT louisdubeau nonsurgicalcancerriskreductioninibrca1imutationcarriersdisablingtheremotecontrol |
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